Zithromax i.v.
Recall
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Medicines
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19/12/2013
In a letter dated December 19, 2013, the marketing authorization holder informed its customers that an elevated level of a known degradation product of the active ingredient azithromycin has been detected in some vials and that a voluntary recall is therefore being carried out. This recall leads to an unavailability of "Zithromax i.v.".
| Name of the medicinal product | Zithromax i.v. 500 mg - Pulver zur Herstellung einer Infusionslösung |
|---|---|
| Marketing authorisation number(s) | 1-24636 |
| Marketing authorisation holder | Pfizer Corporation Austria GmbH |
| Batch number(s) | Z1538 05, Z1894 01, Z2228 03, Z2230 06 |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-0971 |
Further inquiry note
Page last modified:
12/07/2022